| Tag | Content |
|---|
EnhancerAtlas ID | HS076-26851 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr18:45280410-45281360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr18:45281091-45281110 | TGGCGCCCTCTGCTGGTGG | - | 7.59 | | NFAT5 | MA0606.1 | chr18:45280431-45280441 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr18:45280431-45280441 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr18:45280431-45280441 | AATGGAAAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I047754 | chr18 | 45281021 | 45281170 |
|
Enhancer Sequence | CAATTGTTTC TGGCCCAGCC AAATGGAAAA TTTAATTTCC AATTAATTAG CCCTGAATTT 60
GGTGCCCCTC GTCAAGTTAC AGGACTGCCC TTCTCCCAAG AGAGGGGGCT CCCCGCCCAC 120
AGGTGGCCAA CACTTGACAC TGCCTCTGCT GGGAGGGAGA CAAAGGCCCC CAGCCCTGCC 180
ATTGTCTCGG CTCGAGTTCA CGGTCAGGCG GGCACAAAGG CTGGATGAAT TCTTCATGAC 240
CCTCTGAAAG CGTGGCTCTT CCCTATCTGG CCACAGGTGA GCCCTTGAAT GGGGGAGAAG 300
GACATCTTCT CAAGCAGCAA GTGTCCCACC CAACACGGAT CCCAGCCTCC GTCCCCAGCC 360
TCCTGCCCTG GCGCCGCCGC CCCCGCAGTC CGCTGAAACC GGAAGCCCCG GGCCAGTTCA 420
AGACAAGGGC GCCCCGCACC CGGCGCAACT CCCCTCCTTC CACGACACAG CCCTGCTGCT 480
GTGGCATGGC CCTGGCTCTC AGCGGGGCGG TCCCCTTCCC TGCTCCAGAA AGGGTCTCCA 540
GGGCGAGATC TGCCCTGCTT TCCCTTGTAT TAATATAAGG GAAAGTCCTG GGGAGGAAGC 600
TCTCCCCTGC CAGCGTCCAC TCCAGCCTCC AGGAGTCCCT CTCCGCAGGT CTCCATCTTT 660
CCCGCGGGTT CCGCTGTGCT GTGGCGCCCT CTGCTGGTGG GTCCCATGCA GTGCGAGAGT 720
GCTCACCTGG TCCTGGCGTC CTGAAAGCCC ATGTCCCCTA CCTTCAAGTT CCTCCCTCTC 780
CCAAGAAGTC GTTAGAAGGA AGAGGAGGCA GTCCTGTGGC CAGGTCTCTT CTCCAGAGAT 840
AAGTAGAGGA GGGATGAAGA AAAAACAAGG CCTGGGGGAG GGGCTGGGAT TTGAGTTAAT 900
GAGCTATGTA TTTTCCTTTC TCTATAATCC ACGGTATTGG ATGCAGCAGC 950
|
